Khan SG - Search Results

1

Burning issues in the diagnosis of xeroderma pigmentosum.

Kraemer KH, Tamura D, Khan SG, Digiovanna JJ. Kraemer KH, et al. Among authors: khan sg. Br J Dermatol. 2013 Dec;169(6):1176. doi: 10.1111/bjd.12707. Br J Dermatol. 2013. PMID: 24299525 Free PMC article. No abstract available.

2

Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia.

Khan SG, Levy HL, Legerski R, Quackenbush E, Reardon JT, Emmert S, Sancar A, Li L, Schneider TD, Cleaver JE, Kraemer KH. Khan SG, et al. J Invest Dermatol. 1998 Nov;111(5):791-6. doi: 10.1046/j.1523-1747.1998.00391.x. J Invest Dermatol. 1998. PMID: 9804340 Free article.

3

The xeroderma pigmentosum group C gene leads to selective repair of cyclobutane pyrimidine dimers rather than 6-4 photoproducts.

Emmert S, Kobayashi N, Khan SG, Kraemer KH. Emmert S, et al. Among authors: khan sg. Proc Natl Acad Sci U S A. 2000 Feb 29;97(5):2151-6. doi: 10.1073/pnas.040559697. Proc Natl Acad Sci U S A. 2000. PMID: 10681431 Free PMC article.

4

A new xeroderma pigmentosum group C poly(AT) insertion/deletion polymorphism.

Khan SG, Metter EJ, Tarone RE, Bohr VA, Grossman L, Hedayati M, Bale SJ, Emmert S, Kraemer KH. Khan SG, et al. Carcinogenesis. 2000 Oct;21(10):1821-5. doi: 10.1093/carcin/21.10.1821. Carcinogenesis. 2000. PMID: 11023539

5

Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life.

Slor H, Batko S, Khan SG, Sobe T, Emmert S, Khadavi A, Frumkin A, Busch DB, Albert RB, Kraemer KH. Slor H, et al. Among authors: khan sg. J Invest Dermatol. 2000 Dec;115(6):974-80. doi: 10.1046/j.1523-1747.2000.00190.x. J Invest Dermatol. 2000. PMID: 11121128 Free article.

6

The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms.

Emmert S, Schneider TD, Khan SG, Kraemer KH. Emmert S, et al. Among authors: khan sg. Nucleic Acids Res. 2001 Apr 1;29(7):1443-52. doi: 10.1093/nar/29.7.1443. Nucleic Acids Res. 2001. PMID: 11266544 Free PMC article.

7

An intronic poly (AT) polymorphism of the DNA repair gene XPC and risk of squamous cell carcinoma of the head and neck: a case-control study.

Shen H, Sturgis EM, Khan SG, Qiao Y, Shahlavi T, Eicher SA, Xu Y, Wang X, Strom SS, Spitz MR, Kraemer KH, Wei Q. Shen H, et al. Among authors: khan sg. Cancer Res. 2001 Apr 15;61(8):3321-5. Cancer Res. 2001. PMID: 11309287

8

A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: molecular genetic evidence for a common ancestor.

Gozukara EM, Khan SG, Metin A, Emmert S, Busch DB, Shahlavi T, Coleman DM, Miller M, Chinsomboon N, Stefanini M, Kraemer KH. Gozukara EM, et al. Among authors: khan sg. J Invest Dermatol. 2001 Aug;117(2):197-204. doi: 10.1046/j.1523-1747.2001.01424.x. J Invest Dermatol. 2001. PMID: 11511294 Free article.

9

Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.

Emmert S, Slor H, Busch DB, Batko S, Albert RB, Coleman D, Khan SG, Abu-Libdeh B, DiGiovanna JJ, Cunningham BB, Lee MM, Crollick J, Inui H, Ueda T, Hedayati M, Grossman L, Shahlavi T, Cleaver JE, Kraemer KH. Emmert S, et al. Among authors: khan sg. J Invest Dermatol. 2002 Jun;118(6):972-82. doi: 10.1046/j.1523-1747.2002.01782.x. J Invest Dermatol. 2002. PMID: 12060391 Free article.

10

The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function.

Khan SG, Muniz-Medina V, Shahlavi T, Baker CC, Inui H, Ueda T, Emmert S, Schneider TD, Kraemer KH. Khan SG, et al. Nucleic Acids Res. 2002 Aug 15;30(16):3624-31. doi: 10.1093/nar/gkf469. Nucleic Acids Res. 2002. PMID: 12177305 Free PMC article.

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